Mizuuchi K
Cell. 1984 Dec;39(2 Pt 1):395-404. doi: 10.1016/0092-8674(84)90018-7.
The distribution of newly synthesized DNA strands in the transposition products of bacteriophage Mu made in an in vitro system has been analyzed. The results support a model in which all Mu transpositions are initiated by a pair of strand transfer reactions that attach the 3' ends of Mu DNA to 5' protruding staggered ends of the target DNA. Joining of these ends produces a pair of structures similar to replication forks at the ends of the Mu DNA. Successful initiation of replication at either one or both ends, followed by a round of semiconservative replication, results in formation of a cointegrate structure. When the intermediate structure fails to replicate, breakage of the junctions between the Mu sequence and the vector sequence derived from the donor molecule can lead to a simple insert with a pair of gaps at the 5' ends of the Mu DNA. Evidence for a gap repair process that completes the simple insertion process has been obtained.
对在体外系统中产生的噬菌体Mu转座产物中新合成DNA链的分布进行了分析。结果支持这样一种模型,即所有Mu转座均由一对链转移反应启动,该反应将Mu DNA的3'末端连接到靶DNA的5'突出交错末端。这些末端的连接在Mu DNA末端产生一对类似于复制叉的结构。在一端或两端成功启动复制,随后进行一轮半保留复制,导致形成共整合结构。当中间结构无法复制时,Mu序列与来自供体分子的载体序列之间的连接断裂会导致在Mu DNA的5'末端有一对缺口的简单插入。已经获得了完成简单插入过程的缺口修复过程的证据。